U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O10S2
Molecular Weight 352.295
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULMARIN

SMILES

CC1=CC(=O)OC2=C1C=C(OS(O)(=O)=O)C(OS(O)(=O)=O)=C2

InChI

InChIKey=SZNQDPUZKFSCNG-UHFFFAOYSA-N
InChI=1S/C10H8O10S2/c1-5-2-10(11)18-7-4-9(20-22(15,16)17)8(3-6(5)7)19-21(12,13)14/h2-4H,1H3,(H,12,13,14)(H,15,16,17)

HIDE SMILES / InChI

Molecular Formula C10H8O10S2
Molecular Weight 352.295
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulmarin is a water-soluble coumarin derivative with vitamin P activity. In preclinical models Sulmarin facilitates excitatory transmission from parasympathetic fibers to the gastric musculature, increasing acetylcholine release. Sulmarin reduced the tone of isolated calf coronary arteries and also inhibited the contractile response of the arteries to angiotensin II amide (Hypertensin).

Originator

Sources: Farmaco (1946-1952) (1948), 3, 297-300.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Effect of a flavonoid (4-methylesculetin) on the response of isolated calf coronary arteries to histamine].
1977-11-30
Patents

Patents

Substance Class Chemical
Created
by admin
on Wed Apr 02 08:59:15 GMT 2025
Edited
by admin
on Wed Apr 02 08:59:15 GMT 2025
Record UNII
73W96524XT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULMARIN
INN   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
IDRO P2
Preferred Name English
Sulmarin [WHO-DD]
Common Name English
M.G. 143
Code English
SULMARIN [USAN]
Common Name English
SULMARIN [MI]
Common Name English
6,7-Dihydroxy-4-methylcoumarin bis(hydrogen sulfate)
Systematic Name English
sulmarin [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45597
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
Code System Code Type Description
MERCK INDEX
m10384
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY Merck Index
ChEMBL
CHEMBL2104898
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
EVMPD
SUB10747MIG
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
INN
3703
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
PUBCHEM
13963
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
SMS_ID
100000082952
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
DRUG CENTRAL
3573
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
NCI_THESAURUS
C74242
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
ECHA (EC/EINECS)
249-567-8
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
FDA UNII
73W96524XT
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID10183570
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
CAS
29334-07-4
Created by admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY